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Nature|June 9, 1988
The major Fc receptor in blood has a phosphatidylinositol anchor and is deficient in paroxysmal nocturnal haemoglobinuriaP Selvaraj, W F Rosse, R Silber, et al.Blood|February 1, 1978
Differences in the terminal steps of complement lysis of normal and paroxysmal nocturnal hemoglobinuria red cellsT A Rouault, W F Rosse, S Bell, et al.Biochemical and Biophysical Research Communications|January 30, 1990
The homologous restriction factor is immunologically related to complement components C8 and C9 and to lymphocyte pore-forming protein perforin through cysteine-rich domainsJ D Young, W F Rosse, C S Hasselkus-LightJournal of Supramolecular Structure|January 1, 1978
Membrane alterations in irreversibly sickled cells: hemoglobin--membrane interactionL S Lessin, J Kurantsin-Mills, C Wallas, et al.Annals of Internal Medicine|April 1, 1975
Resolution of primary amyloidosis during chemotherapy. Studies in a patient with nephrotic syndromeH J Cohen, L S Lessin, J Hallal, et al.American Journal of Hematology|July 1, 1993
High Ia (HLA-DR) and low CD11b (Mo1) expression may predict early conversion to leukemia in myelodysplastic syndromesM Mittelman, D S Karcher, L A Kammerman, et al.The American Journal of Medicine|October 1, 1975
Multiple myeloma in a patient with sickel cell anemia. Interacting effects on blood viscosityI S Anderson, K Y Yeung, D Hillman, et al.Journal of Immunology (Baltimore, Md. : 1950)|June 1, 1989
Distinct restriction of complement- and cell-mediated lysisN Hollander, M L Shin, W F Rosse, et al.The Journal of Clinical Investigation|June 1, 1985
Characterization of the complement sensitivity of paroxysmal nocturnal hemoglobinuria erythrocytesC J Parker, T Wiedmer, P J Sims, et al.American Journal of Hematology|April 1, 1990
Pulmonary embolism and splenic infarction in a patient with sickle cell traitJ Sugarman, W M Samuelson, R H Wilkinson, et al.Pageof 14